C. Nuttin

807 total citations
12 papers, 527 citations indexed

About

C. Nuttin is a scholar working on Molecular Biology, Cognitive Neuroscience and Clinical Biochemistry. According to data from OpenAlex, C. Nuttin has authored 12 papers receiving a total of 527 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Cognitive Neuroscience and 3 papers in Clinical Biochemistry. Recurrent topics in C. Nuttin's work include Metabolism and Genetic Disorders (3 papers), Mitochondrial Function and Pathology (2 papers) and Epilepsy research and treatment (2 papers). C. Nuttin is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Mitochondrial Function and Pathology (2 papers) and Epilepsy research and treatment (2 papers). C. Nuttin collaborates with scholars based in France, Belgium and Luxembourg. C. Nuttin's co-authors include Catherine Chiron, A. Syrota, Fernando Gordillo León, Jean Marie Saudubray, Marion Leboyer, Emmanuel Scalais, Olivier Dulac, Gisèle Depas, Claude Raynaud and Françis Brunelle and has published in prestigious journals such as Epilepsia, Developmental Medicine & Child Neurology and Epilepsy Research.

In The Last Decade

C. Nuttin

11 papers receiving 510 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
C. Nuttin France	11	189	125	118	97	95	12	527
Raffaello Canapicchi Italy	12	120 0.6×	58 0.5×	97 0.8×	253 2.6×	161 1.7×	20	628
Pilar Póo Spain	17	187 1.0×	101 0.8×	130 1.1×	206 2.1×	155 1.6×	34	688
Anita Devlin United Kingdom	9	126 0.7×	55 0.4×	63 0.5×	210 2.2×	268 2.8×	28	595
Santosh Mordekar United Kingdom	16	121 0.6×	73 0.6×	48 0.4×	125 1.3×	175 1.8×	48	655
Jeehun Lee South Korea	17	204 1.1×	43 0.3×	132 1.1×	219 2.3×	250 2.6×	80	855
Daniel Kenney‐Jung United States	15	190 1.0×	108 0.9×	71 0.6×	117 1.2×	302 3.2×	36	700
T Deonna Switzerland	14	180 1.0×	104 0.8×	31 0.3×	174 1.8×	212 2.2×	29	702
Roelineke J. Lunsing Netherlands	18	269 1.4×	26 0.2×	178 1.5×	188 1.9×	95 1.0×	35	679
Shin Okazaki Japan	12	243 1.3×	50 0.4×	38 0.3×	66 0.7×	148 1.6×	79	620
Gilles Lyon Belgium	13	119 0.6×	45 0.4×	49 0.4×	160 1.6×	109 1.1×	18	515

Countries citing papers authored by C. Nuttin

Since Specialization

Citations

This map shows the geographic impact of C. Nuttin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by C. Nuttin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Nuttin more than expected).

Fields of papers citing papers by C. Nuttin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. Nuttin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by C. Nuttin. The network helps show where C. Nuttin may publish in the future.

Co-authorship network of co-authors of C. Nuttin

This figure shows the co-authorship network connecting the top 25 collaborators of C. Nuttin. A scholar is included among the top collaborators of C. Nuttin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C. Nuttin. C. Nuttin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Scalais, Emmanuel, Rudy Van Coster, L. Bindl, et al.. (2013). Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2). European Journal of Paediatric Neurology. 17(6). 625–630. 47 indexed citations

Scalais, Emmanuel, Baudouin François, René Stevens, et al.. (2012). Polymerase gamma deficiency (POLG): Clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh’s encephalopathy. European Journal of Paediatric Neurology. 16(5). 542–548. 16 indexed citations

Gataullina, Svetlana, Perrine Plouin, Angela Vincent, et al.. (2011). Paroxysmal EEG pattern in a child with N-methyl-d-aspartate receptor antibody encephalitis. Developmental Medicine & Child Neurology. 53(8). 764–767. 12 indexed citations

Roels, Frank, Marianne Depreter, M. Girós, et al.. (2002). Differential organ involvement in peroxisomal disorders. Journal of Inherited Metabolic Disease. 25. 99–99.

Scalais, Emmanuel, et al.. (1998). Multimodality evoked potentials as a prognostic tool in term asphyxiated newborns. Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section. 108(2). 199–207. 33 indexed citations

Chiron, Catherine, Rima Nabbout, Florence Pinton, et al.. (1996). Brain functional imaging SPECT in agyria-pachygyria. Epilepsy Research. 24(2). 109–117. 10 indexed citations

Chiron, Catherine, et al.. (1995). SPECT OF THE BRAIN IN CHILDHOOD AUTISM: EVIDENCE FOR A LACK OF NORMAL HEMISPHERIC ASYMMETRY. Developmental Medicine & Child Neurology. 37(10). 849–860. 113 indexed citations

Dubois, Josée, Françis Brunelle, Guy Touati, et al.. (1995). Hyperinsulinism in children: Diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases. Pediatric Radiology. 25(7). 512–516. 86 indexed citations

Depas, Gisèle, Catherine Chiron, Marc Tardieu, et al.. (1995). Functional brain imaging in HIV-1-infected children born to seropositive mothers.. PubMed. 36(12). 2169–74. 21 indexed citations

10.

Chiron, Catherine, Olivier Dulac, Christine Bulteau, et al.. (1993). Study of Regional Cerebral Blood Flow in West Syndrome. Epilepsia. 34(4). 707–715. 58 indexed citations

11.

Mitchell, G. H., Jean‐Paul Bonnefont, Gary J. Schwartz, et al.. (1992). Approach to the patient with a fatty acid oxidation disorder.. PubMed. 375. 271–88. 14 indexed citations

12.

Münnich, Arnold, Pierre Rustin, Agnès Rötig, et al.. (1992). Clinical aspects of mitochondrial disorders. Journal of Inherited Metabolic Disease. 15(4). 448–455. 117 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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